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FDA 510(k)

CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC.

K-Number: K803022 · 1980-12-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1980-12-22
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC. is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K803022. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC.?

CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC. is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K803022.

When did CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC. receive FDA 510(k) clearance?

CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC. received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803022.

Who is the listed applicant for CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC.?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC.?

The FDA product code for CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC. is JSJ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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